NCT06964880

Brief Summary

Sarcopenic obesity refers to a condition characterized by high body fat percentage and insufficient muscle mass, posing significant risks to physical and mental health. This issue is not limited to the elderly; it is increasingly common among younger populations as well. According to the National Nutrition and Health Survey conducted between 2017 and 2020, high rates of eating out due to study and work lifestyles in Taiwan result in limited access to nutritious food. The Ministry of Health and Welfare's statistics from 2021 show that only 33.9% of the population engages in regular exercise. Sarcopenic obesity is associated with physical activity and nutritional intake. The European Working Group on Sarcopenia in Older People has urged the public to maintain a balanced diet and establish exercise habits early to reduce the risk of sarcopenic obesity. Younger individuals are more likely to increase muscle mass with interventions in exercise and nutrition compared to older adults, making college students a key demographic for fostering healthy behaviors. Therefore, it is essential to address how to enhance their health awareness and behaviors. Based on this, the present study aims to explore the impact of a multimedia intervention combined with a peer support model on the awareness and behaviors of college students at risk of being overweight. The research methodology involves a randomized controlled trial, participants from a medical university in central Taiwan. Body composition will be measured first, and eligible participants will be randomly assigned to either an experimental group or a control group, followed by a 12-week intervention and subsequent post-test. The study will analyze the effects of multimedia combined with peer support on the awareness and behaviors of at-risk college students, as well as assess muscle mass changes through grip strength measurements. The goal is to enhance college students' awareness of their health behaviors, improve their dietary and exercise habits, fill knowledge and application gaps, and provide an evidence-based foundation for future strategies to promote healthy behaviors among young populations.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started May 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 4, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

May 1, 2025

Completed
10 days until next milestone

First Posted

Study publicly available on registry

May 11, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
Last Updated

May 11, 2025

Status Verified

May 1, 2025

Enrollment Period

5 months

First QC Date

March 4, 2025

Last Update Submit

May 7, 2025

Conditions

Keywords

Sarcopenic obesitybody fat percentagemuscle massexerciseaudiovisual media

Outcome Measures

Primary Outcomes (4)

  • Body Mass Index (BMI)

    BMI will be calculated as weight (kg) divided by height in meters squared (m²). Measurements will be taken using the InBody 270S body composition analyzer. Unit of Measure: kg/m²

    From enrollment to the end of treatment at 12 weeks

  • Body Fat Percentage Body fat mass

    Body Fat Percentage Body fat mass will be assessed using the InBody 270S. Percentage is calculated as (fat mass ÷ body weight (kg)) × 100%. Unit of Measure: %

    From enrollment to the end of treatment at 12 weeks

  • Physical Activity Level (IPAQ-SF)

    Assessed using the International Physical Activity Questionnaire - Short Form (IPAQ-SF). Results expressed in MET-minutes/week. Higher scores indicate greater physical activity and better outcome. Unit of Measure: MET-min/week

    From enrollment to the end of treatment at 12 weeks

  • Hand Grip Strength

    Hand grip strength measured using Jamar handheld dynamometer. Each hand is tested three times; average grip strength is recorded. Higher values indicate better strength. Unit of Measure: kg

    From enrollment to the end of treatment at 12 weeks

Study Arms (2)

Online Video Exercise + Peer Support

EXPERIMENTAL

Participants in the intervention group will engage in a 12-week program that includes twice-weekly structured exercise sessions guided by video content delivered via an online media platform. The program also includes weekly health education videos on nutrition and sarcopenic obesity. Participants will be organized into peer support groups (5 members per group) to promote mutual encouragement and accountability in maintaining healthy behaviors.

Behavioral: Exercise with video on media platform

Printed Health Education Materials

ACTIVE COMPARATOR

Participants in the control group will receive printed health education materials weekly for 12 weeks. These materials cover the same topics as the intervention group, including healthy eating, physical activity, and prevention of sarcopenic obesity, but without the video-based guidance or peer group support.

Behavioral: Printed Educational Handout

Interventions

12-week structured video-guided exercise and peer support program

Online Video Exercise + Peer Support

12-week printed health education handout program

Printed Health Education Materials

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Undergraduate students in years 1 to 4 at a medical university in central Taiwan
  • Body Mass Index (BMI) between 23 and 27 or body fat percentage between 25% and 35%
  • Aged 18 to 25 years
  • No diagnosis of any chronic disease

You may not qualify if:

  • University students with restricted limb movement who are unable to exercise according to instructions.
  • Any condition that may restrict the proper use of a dynamometer (e.g., hand pain, osteoarthritis, or rheumatoid arthritis).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ya-Ling Tzeng

Taichung, 406040, Taiwan

RECRUITING

MeSH Terms

Conditions

Motor Activity

Interventions

Exercise

Condition Hierarchy (Ancestors)

Behavior

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Ya-Ling Tzeng, PhD

    China Medical University, Taiwan

    STUDY DIRECTOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 4, 2025

First Posted

May 11, 2025

Study Start

May 1, 2025

Primary Completion

September 30, 2025

Study Completion

December 31, 2025

Last Updated

May 11, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

Locations